A Novel Antagonist Peptide Reveals a Physiological Role of Insulin-Like Peptide 5 in Control of Colorectal Function

Autor: John B. Furness, Praveen Praveen, Mohammed Akhter Hossain, Shuai Nie, Qinghao Ou, Ruslan V Pustovit, Jamie Jm Liew, Xiaozhou Zhang, Martina Kocan, Lalita Oparija-Rogenmozere, Mengjie Liu, Ada Koo, Ross A. D. Bathgate
Rok vydání: 2021
Předmět:
Zdroj: ACS Pharmacol Transl Sci
ISSN: 2575-9108
DOI: 10.1021/acsptsci.1c00171
Popis: [Image: see text] Insulin-like peptide 5 (INSL5), the natural ligand for the relaxin family peptide receptor 4 (RXFP4), is a gut hormone that is exclusively produced by colonic L-cells. We have recently developed an analogue of INSL5, INSL5-A13, that acts as an RXFP4 agonist in vitro and stimulates colorectal propulsion in wild-type mice but not in RXFP4-knockout mice. These results suggest that INSL5 may have a physiological role in the control of colorectal motility. To investigate this possibility, in this study we designed and developed a novel INSL5 analogue, INSL5-A13NR. This compound is a potent antagonist, without significant agonist activity, in two in vitro assays. We report here for the first time that this novel antagonist peptide blocks agonist-induced increase in colon motility in mice that express RXFP4. Our data also show that colorectal propulsion induced by intracolonic administration of bacterial products (short-chain fatty acids, SCFAs) is antagonized by INSL5-A13NR. Therefore, INSL5-A13NR is an important research tool and potential drug lead for the treatment of colon motility disorders, such as bacterial diarrheas.
Databáze: OpenAIRE